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正常鼠肾对高盐摄入的代谢反应。

Metabolic Responses of Normal Rat Kidneys to a High Salt Intake.

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

Mass Spectrometry and Protein Chemistry, Protein Sciences, The Jackson Laboratory, Bar Harbor, ME 04609, USA.

出版信息

Function (Oxf). 2023 Jun 22;4(5):zqad031. doi: 10.1093/function/zqad031. eCollection 2023.

Abstract

In this study, novel methods were developed, which allowed continuous (24/7) measurement of arterial blood pressure and renal blood flow in freely moving rats and the intermittent collection of arterial and renal venous blood to estimate kidney metabolic fluxes of O and metabolites. Specifically, the study determined the effects of a high salt (HS; 4.0% NaCl) diet upon whole kidney O consumption and arterial and renal venous plasma metabolomic profiles of normal Sprague-Dawley rats. A separate group of rats was studied to determine changes in the cortex and outer medulla tissue metabolomic and mRNAseq profiles before and following the switch from a 0.4% to 4.0% NaCl diet. In addition, targeted mRNA expression analysis of cortical segments was performed. Significant changes in the metabolomic and transcriptomic profiles occurred with feeding of the HS diet. A progressive increase of kidney O consumption was found despite a reduction in expression of most of the mRNA encoding enzymes of TCA cycle. A novel finding was the increased expression of glycolysis-related genes in Cx and isolated proximal tubular segments in response to an HS diet, consistent with increased release of pyruvate and lactate from the kidney to the renal venous blood. Data suggests that aerobic glycolysis (eg, Warburg effect) may contribute to energy production under these circumstances. The study provides evidence that kidney metabolism responds to an HS diet enabling enhanced energy production while protecting from oxidative stress and injury. Metabolomic and transcriptomic analysis of kidneys of Sprague-Dawley rats fed a high salt diet.

摘要

在这项研究中,开发了新的方法,允许在自由活动的大鼠中连续(24/7)测量动脉血压和肾血流量,并间歇性采集动脉和肾静脉血液以估计肾脏的 O 和代谢物代谢通量。具体来说,该研究确定了高盐(HS;4.0%NaCl)饮食对正常 Sprague-Dawley 大鼠的整个肾脏 O 消耗以及动脉和肾静脉血浆代谢组学图谱的影响。另一组大鼠被研究以确定在从 0.4%NaCl 饮食转换为 4.0%NaCl 饮食之前和之后,皮质和外髓质组织代谢组学和 mRNAseq 图谱的变化。此外,还对皮质段的靶向 mRNA 表达分析进行了研究。随着 HS 饮食的摄入,代谢组学和转录组学图谱发生了显著变化。尽管大多数编码 TCA 循环酶的 mRNA 的表达减少,但发现肾脏 O 消耗呈渐进性增加。一个新的发现是,在 HS 饮食的刺激下,Cx 和分离的近端肾小管段中与糖酵解相关的基因表达增加,这与肾脏向肾静脉血液中释放丙酮酸和乳酸增加一致。数据表明,在这些情况下,有氧糖酵解(例如,Warburg 效应)可能有助于能量产生。该研究为肾脏代谢对 HS 饮食的反应提供了证据,从而能够增强能量产生,同时防止氧化应激和损伤。高盐饮食喂养的 Sprague-Dawley 大鼠肾脏的代谢组学和转录组学分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4102/10413938/932d7a730d65/zqad031fig1g.jpg

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